期刊文献+

介孔炭的直接制备及其电化学性能研究 被引量:3

Direct Preparation of Mesoporous Carbons and Their Electrochemical Performances
下载PDF
导出
摘要 以柠檬酸镁为原料,采用直接碳化法制备介孔炭电极材料。N2吸附测试表明,所制备多孔炭的比表面积达2 000 m2·g-1左右,介孔孔容和平均孔径随着炭化温度的升高而增加,当炭化温度大于800℃时,能够制备出以介孔结构为主的多孔炭材料。电化学测试表明,MgC-800和MgC-900具有优异的电化学电容特性。与硬模板法制备的OMC相比,MgC-800和MgC-900在实验电流密度范围内具有更大的比电容值,这应当归功于它们巨大的比表面积以及有利于电解质离子扩散的介孔结构。 Mesoporous electrode materials were prepared directly from magnesium citrate.N2 adsorption shows that the specific surface area of the porous carbons prepared amounts to approximate 2 000 m^2·g^-1,and that mesopore size and volume increase with the rise of carbonization temperature.Typical meso-structured porous carbon can be prepared when carbonization temperature is higher than 800 ℃.Electrochemical measurements demonstrate that MgC-800 and MgC-900 possess good capacitive behavior.Compared to hard-templated OMC,MgC-800 and MgC-900 have lager specific capacitance within the applied current densities in this work,which can be ascribed to their large surface area and mesoporous structure that favors fast electrolyte diffusion in the pore channels.
出处 《无机化学学报》 SCIE CAS CSCD 北大核心 2011年第2期219-225,共7页 Chinese Journal of Inorganic Chemistry
基金 山东省自然科学基金(No.Y2007B29 Y2008F36) 山东省中青年科学家科研奖励基金(No.2008BS09007) 山东省科技专项基金(No.2006GG1108097-04)资助项目
关键词 超级电容器 电化学 介孔炭 电极材料 supercapacitor electrochemistry mesoporous carbon electrode material
  • 相关文献

参考文献26

  • 1Service R F.Science,2006,313:902-905.
  • 2Kandalkar S G,Lokhande C D,Mane R S,et al.Appl.Surf.Sci.,2007,253:3952-3956.
  • 3Xu C J,Li B H,Du H D,et al.J.Power Sources,2008,184:691-694.
  • 4HUANGJian-Hua(黄建华) LAIQiong-Yu(赖琼钰) SONGJian-Mei(宋建梅) etal.Wuji Huaxue Xuebao,2007,23:237-242.
  • 5Fonseca C P,Benedetti J E,Neves S.J.Power Sources,2006,158:789-794.
  • 6Girija T C,Sangaranarayanan M V.Synth.Metals,2006,156:244-250.
  • 7LILi-Min(李利民) LIUEn-Hui(刘恩辉) LIJian(李剑) etal.Wuli Huaxue Xuebao,2010,26:1521-1526.
  • 8JIANGQi(江奇) QuMei-Zhen(瞿美臻) ZHANGBo-Lan(张伯兰) etal.Wuji Cailiao Xuebao,2002,17:651-656.
  • 9Centeno T A,Stoeckli F.Electrochim.Acta,2006,52:560-566.
  • 10Leitner K,Left A,Winter M,et al.J.Power Sources,2006,153:419-423.

同被引文献19

  • 1Choi N S, Chen Z H, Freunberger S A, et al. Angew. Chem. Int. Ed., 2012,51:9994-10024.
  • 2Liu C, Li F, Ma L P, et al. Adv. Mater., 2010,22:28-62.
  • 3Xia K S, Gao Q M, Jiang J H, et al. Carbon, 2008,46:1718-1726.
  • 4Stoller M D, Park S J, Zhu Y W, et al. Nano Lett., 2008,8: 3498-3502.
  • 5Zhai Y P, Dou Y Q, Zhao D Y, et al. Adv. Mater., 2011,23: 4828-4850.
  • 6Ye H, Cheng Y W, Hobson T, et al. Nano Lett., 2010,10: 2727-2733.
  • 7Noked M, Soffer A, Aurbach D. J. Solid State Electrochem., 2011,15:1563-1578.
  • 8Xie K, Qing X T, Wang X Z, et al. Adv. Mater., 2012,24: 347-352.
  • 9Stein A, Wang Z Y, Fierke M A, et al. Adv. Mater., 2009,21:265-293.
  • 10Lang J W, Yan X B, Liu W W, et al. J. Power Sources, 2012,204:220-229.

引证文献3

二级引证文献8

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部